Canonical Allele Identifier: CA442332832

Gene: AGA

Linked Data

• MyVariant Identifiers: chr4:g.178360803T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.177439649T>G , CM000666.2:g.177439649T>G	GRCh38
NC_000004.11:g.178360803T>G , CM000666.1:g.178360803T>G	GRCh37
NC_000004.10:g.178597797T>G	NCBI36
NG_011845.2:g.7855A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000264595.7:c.321A>C MANE Select	ENSP00000264595.2:p.Arg107=
ENST00000264595.6:c.321A>C	ENSP00000264595.2:p.Arg107=
ENST00000506853.5:n.355A>C
ENST00000510635.1:c.17A>C
ENST00000510955.5:n.315+624A>C
NM_000027.3:c.321A>C	NP_000018.2:p.Arg107=
NM_001171988.1:c.321A>C	NP_001165459.1:p.Arg107=
NR_033655.1:n.449A>C
XM_006714123.2:c.321A>C	XP_006714186.1:p.Arg107=
XR_001741155.2:n.415A>C
NM_000027.4:c.321A>C MANE Select	NP_000018.2:p.Arg107=
NM_001171988.2:c.321A>C	NP_001165459.1:p.Arg107=
NR_033655.2:n.383A>C